TF, transferrin, 7018

N. diseases: 168; N. variants: 74
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		phenotype Laboratory Procedure 6 10 0.100 None 1.000 3 3 2011 2015
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		phenotype Laboratory Procedure 6 10 0.100 None 1.000 3 3 2011 2015
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		phenotype Clinical Attribute 20 35 0.100 None 1.000 3 5 2011 2017
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		phenotype Finding 653 1206 0.100 None 1.000 3 5 2016 2019
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		phenotype Laboratory Procedure 20 35 0.100 None 1.000 3 5 2011 2017
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		phenotype Laboratory Procedure 593 988 0.100 None 1.000 2 2 2016 2019
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		phenotype Laboratory Procedure 26 36 0.100 None 1.000 2 3 2014 2017
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		phenotype Laboratory or Test Result 593 988 0.100 None 1.000 2 2 2016 2019
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		phenotype Laboratory Procedure 17 25 0.100 None 1.000 2 2 2014 2015
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		phenotype Laboratory or Test Result 401 4389 0.100 None 1.000 2 3 2016 2018
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		phenotype Laboratory Procedure 717 1599 0.100 None 1.000 1 1 2019 2019
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		phenotype Laboratory Procedure 483 1142 0.100 None 1.000 1 1 2012 2012
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		disease Disease or Syndrome 23 2 0.010 None 1.000 1 2017 2017
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis 		disease Disease or Syndrome 40 0.010 None 1.000 1 2004 2004
CUI: C0337439
Disease: Iron measurement
Iron measurement 		phenotype Laboratory Procedure 12 16 0.100 None 1.000 1 1 2011 2011
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		phenotype Laboratory Procedure 269 555 0.100 None 1.000 1 1 2012 2012
CUI: C0428578
Disease: Iron level result
Iron level result 		phenotype Laboratory or Test Result 12 16 0.100 None 1.000 1 1 2011 2011
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		phenotype Laboratory or Test Result 269 549 0.100 None 1.000 1 3 2016 2016
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease 		phenotype Neoplastic Process 384 40 0.010 None 1.000 1 2013 2013
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 1 2018 2018
CUI: C3277918
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 		phenotype Finding 1 0.200 None 1.000 1 1987 1987
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD 		disease Disease or Syndrome 384 40 0.010 None 1.000 1 2013 2013
CUI: C3889615
Disease: TRANSFERRIN VARIANT D1 PHENOTYPE
TRANSFERRIN VARIANT D1 PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C3889617
Disease: TRANSFERRIN VARIANT B2 PHENOTYPE
TRANSFERRIN VARIANT B2 PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C3889619
Disease: TRANSFERRIN VARIANT Bv PHENOTYPE
TRANSFERRIN VARIANT Bv PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1